Literature DB >> 19885090

Parenteral glucose and glucose control in the critically ill: a kinetic appraisal.

Roman Hovorka1, Jeremy Cordingley.   

Abstract

BACKGROUND: We investigated the influence of parenteral glucose infusion on insulin-driven tight glucose control (4.4-6.1 mmol/liter) in the critically ill by appraising kinetic characteristics of the glucoregulatory system.
METHODS: Turnover characteristics of the glucoregulatory system associated with constant 0, 1.2, and 2.4 mg/kg/min parenteral glucose infusion were obtained by literature review and mass-balance calculations.
RESULTS: Without parenteral glucose infusion, the achievement of tight glucose control is hampered by long time delays with an anticipated glucose equilibration half-time (T((1/2))) of 185 min. The constant parenteral glucose infusions of 1.2 and 2.4 mg/kg/min reduce T((1/2)) to 80 and 40 min, respectively. This follows on from the accelerated glucose turnover brought about by the insulin-modulated glucose uptake, which increases in response to increasing exogenous insulin required to achieve tight glucose control. However, large variations exist among glucose turnover characteristics in the critically ill.
CONCLUSIONS: The constant parenteral glucose infusion greater or equal to 2.4 mg/kg/min is expected to simplify the achievement of tight glucose control by reducing system delays and may facilitate the development of more intuitive, efficacious, and safer insulin-titration guidelines.

Entities:  

Keywords:  critical illness; glucose control; glucose metabolism; insulin titration; kinetic analysis; parenteral nutrition

Year:  2007        PMID: 19885090      PMCID: PMC2769589          DOI: 10.1177/193229680700100307

Source DB:  PubMed          Journal:  J Diabetes Sci Technol        ISSN: 1932-2968


  35 in total

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Review 2.  Nutrition support in clinical practice: review of published data and recommendations for future research directions. National Institutes of Health, American Society for Parenteral and Enteral Nutrition, and American Society for Clinical Nutrition.

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3.  Rates and tissue sites of non-insulin- and insulin-mediated glucose uptake in humans.

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4.  Partitioning glucose distribution/transport, disposal, and endogenous production during IVGTT.

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